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EP0636652A1 - Masse à mouler thermoplastique d'un copolymère à base d'alkylesters d'acide méthacrylique et un copolymère greffé à cinq étapes en émulsion - Google Patents

Masse à mouler thermoplastique d'un copolymère à base d'alkylesters d'acide méthacrylique et un copolymère greffé à cinq étapes en émulsion Download PDF

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Publication number
EP0636652A1
EP0636652A1 EP94111540A EP94111540A EP0636652A1 EP 0636652 A1 EP0636652 A1 EP 0636652A1 EP 94111540 A EP94111540 A EP 94111540A EP 94111540 A EP94111540 A EP 94111540A EP 0636652 A1 EP0636652 A1 EP 0636652A1
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EP
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Prior art keywords
weight
obtainable
shell
monomer mixture
essentially
Prior art date
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Application number
EP94111540A
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German (de)
English (en)
Inventor
Andreas Dr. Deckers
Daniel Dr. Wagner
Reiner Wanzek
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BASF SE
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BASF SE
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
    • C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
    • C08F265/06—Polymerisation of acrylate or methacrylate esters on to polymers thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C08F212/02—Monomers containing only one unsaturated aliphatic radical
    • C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
    • C08F212/06—Hydrocarbons
    • C08F212/08—Styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10—Esters
    • C08F220/12—Esters of monohydric alcohols or phenols
    • C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F285/00—Macromolecular compounds obtained by polymerising monomers on to preformed graft polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2351/00—Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers

Definitions

  • the invention relates to a process for producing the thermoplastic molding compositions according to the invention, their use and molded articles and films produced therefrom.
  • EP-A 512 333 describes thermoplastic compositions which contain 5 to 65% by weight of the emulsion graft copolymer (B) used according to the invention to improve the impact strength.
  • the thermoplastic materials mentioned in the above-mentioned EP laid-open specification cannot be processed into low-break films.
  • the object of the present invention was therefore to provide further thermoplastic molding compositions which can be processed to give low-whitening films.
  • thermoplastic molding compositions defined at the outset are thermoplastic molding compositions defined at the outset.
  • thermoplastic compositions Furthermore, a process for their production, their use for the production of moldings and films, and moldings and films made from these thermoplastic compositions have been found.
  • thermoplastic molding compositions according to the invention essentially contain 20 to 40% by weight, preferably 20 to 34.99% by weight, of a copolymer, essentially obtainable from 80 to 100 wt .-%, preferably 90 to 99 wt .-%, at least one C1-C18 alkyl ester of methacrylic acid and 0 to 20 wt .-%, preferably 1 to 10 wt .-%, of at least one C1-C18 alkyl ester of acrylic acid and 60 to 80 wt .-%, preferably 65.01 to 80 wt .-%, a five-stage a hard, non-elastomeric core (b1), an elastomeric, first shell (b2), a hard, non-elastomeric, second shell (b3), an elastomeric, third shell (b4) and finally an outer, hard, non-elastomeric, fourth shell (b5) of built-up graft copolymer ⁇ , the individual stages being present in
  • C1-C18 alkyl esters of methacrylic acid are preferably the C1-C4 alkyl esters such as methyl methacrylate (“MMA”), ethyl methacrylate, n-, i-propyl methacrylate, n-butyl methacrylate, isobutyl methacrylate and tert-butyl methacrylate, with methyl methacrylate being particularly preferred, and mixtures of these monomers.
  • MMA methyl methacrylate
  • ethyl methacrylate ethyl methacrylate
  • n- ethyl methacrylate
  • i-propyl methacrylate n-butyl methacrylate
  • isobutyl methacrylate and tert-butyl methacrylate isobutyl methacrylate and tert-butyl methacrylate
  • C1-C18 alkyl esters of acrylic acid use is preferably made of the C1-C4 alkyl esters such as methyl acrylate ("MA"), ethyl acrylate, n-, i-propyl acrylate, n-butyl acrylate, isobutyl acrylate, tert-butyl acrylate, pentyl, hexyl , Heptyl, octyl, 2-ethylhexyl, nonyl, decyl, lauryl or stearyl acrylate, with methyl acrylate, n-butyl acrylate and 2-ethylhexyl acrylate being particularly preferred, and mixtures of these monomers.
  • MA methyl acrylate
  • ethyl acrylate ethyl acrylate
  • n- n-
  • i-propyl acrylate n-butyl acrylate
  • isobutyl acrylate
  • Component A) is generally prepared by known polymerization processes, such as bulk, solution, emulsion or bead polymerization. Such processes are described, for example, in the Kunststoff Handbuch, Vol. 9, Vieweg and Esser; Polymethyl methacrylate, Carl-Hanser-Verlag, Kunststoff 1975, pp. 36 ff.
  • the hard core (b1) of the emulsion graft copolymer consists essentially of the invention 80 to 99.99% by weight, preferably 90 to 98.99% by weight of methyl methacrylate (I), 0.01 to 5% by weight of allyl methacrylate (II), 0 to 19.99% by weight, preferably 1 to 9.99% by weight, of further monofunctional comonomers (III) and 0 to 3% by weight of further di- or polyfunctional comonomers (IV).
  • monofunctional comonomers (III) C1-C20-alkyl acrylate and -C5-C12-cycloalkyl ester, C2-C20-alkyl methacrylate and -C5-C12-cycloalkyl ester, acrylonitrile and methacrylonitrile, acrylic and methacrylamide as well as their N-alkyl and dialkyl derivatives with C1- C20-alkyl groups, vinyl esters of aliphatic C2-C8-carboxylic acids such as vinyl acetate, vinyl aromatics such as styrene, ⁇ -methylstyrene and vinyltoluene, vinyl halides such as vinyl chloride and vinylidene chloride and mixtures of these monomers.
  • acrylic acid-C1-C8-alkyl esters are preferred, in particular acrylic acid ethyl esters, which are preferably contained in an amount of 1 to 6 wt .-% in the polymer of the core.
  • the comonomers (III) serve mainly to improve the thermal stability of the graft copolymers.
  • Alkylene glycol dimethacrylics such as ethylene glycol dimethacrylate, propylene glycol dimethacrylate, 1,3-butylene glycol dimethacrylate and 1,4-butylene glycol dimethacrylate
  • Alkylene glycol diacrylates such as ethylene glycol diacrylate, propylene glycol diacrylate, 1,3-butylene glycol diacrylate and 1,4-butylene glycol diacrylate
  • Acrylates and methacrylates of glycerol, trimethylolpropane, pentaerythritol, inositol and similar sugar alcohols Acrylic and methacrylamides of ethylenediamine and other aliphatic di- and polyamines, Triacryl- and trimethacrylamides, Triallyl cyanurate and triallyl isocyanurate as well Called vinylbenzenes such as divinylbenzene and trivinylbenzene.
  • the comonomers (IV) serve as crosslinking agents. They are also referred to as "polymerization crosslinkers" because of their property of being incorporated evenly into the polymeric phase. During the polymerization reaction, the rate of their consumption is essentially comparable to that of the main monomer, which results in crosslinking within the phase.
  • the comonomers (IV) can be up to 3% by weight in the core polymer, but they are preferably not used with or only in amounts of 0.1 to 0.5% by weight.
  • allyl methacrylate (II) is involved according to the invention with 0.01 to 5% by weight in the structure of the core, the amount being dependent on the desired core size.
  • the proportion of allyl methacrylate is 0.1 to 0.5% by weight.
  • Graft-active comonomers usually ensure external crosslinking and, for example, when the emulsion graft copolymer is built up, they link the core phase with the subsequent polymerization stage.
  • Graft crosslinkers such as allyl methacrylate generally exhibit this behavior because a polymerizable double bond (double bond of the acid part) polymerizes at a rate comparable to that of the main monomer (methyl methacrylate).
  • the double bond of the allyl group reacts with a significantly lower rate of polymerization, so that at the end of the polymerization some of these double bonds remain unchanged in the core phase, which enables graft crosslinking between two phases.
  • the core material usually has a glass transition temperature of more than 50 ° C, which is preferably in the range of 80 to 130 ° C.
  • core latex also called “core latex” or “seed latex”
  • a monomer mixture consisting essentially of 60 to 89.99% by weight, preferably 70 to 89.99% by weight of a C1-C20 alkyl ester of acrylic acid (V), 10 to 39.99% by weight, preferably 10 to 29.99% by weight, of a vinyl aromatic monomer (VI), 0.01 to 5% by weight, preferably 0.1 to 5% by weight of allyl methacrylate (II), 0 to 10 wt .-%, methyl methacrylate (I) and / or a monofunctional comonomer (III) and 0 to 3% by weight of a di- or polyfunctional comonomer (IV), polymerized, which forms the first elastomeric shell (b2) of the five-stage emulsion graft copolymer.
  • the C2-C10 alkyl esters are preferred, with n-butyl acrylate and 2-ethylhexyl acrylate being particularly preferred.
  • Suitable vinyl aromatic monomers (VI) are Styrene ⁇ -methylstyrene, t-butylstyrene, Monochlorostyrene, Vinyl toluene and Phenyl acrylate and methacrylic acid.
  • the vinyl aromatic monomers (VI), in particular styrene, are of particular importance since they increase the refractive index. In this way, it can be compared to that of the core phase and the subsequent polymer phases.
  • the refractive index can also be matched to that of the thermoplastic molding composition by means of the vinyl aromatic monomers of the five-stage emulsion polymer.
  • the polymeric material of the first shell contains 0.01 to 5% by weight, preferably 0.1 to 5% by weight, of the graft crosslinking agent allyl methacrylate (II).
  • the graft crosslinking agent allyl methacrylate (II) allyl methacrylate
  • Their proportion can be 0 to 3% by weight of the total weight of the monomers of the first shell.
  • the proportion of monofunctional comonomers (I) and (III) can be 0 to 10% by weight, it being so limited that the glass transition temperature of 0 ° C in the elastomeric first shell is not exceeded.
  • monofunctional comonomers III Vinyl carbazole Maleic, fumaric and itaconic acid-C1 to C10 alkyl esters, maleic, fumaric and itaconic acid amide and their N-alkyl and N, N-dialkyl derivatives with C1 to C1 C alkyl groups.
  • Strongly polar monofunctional comonomers (III) such as Acrylic and methacrylic acid, Acrylic and methacrylamides, Hydroxyalkyl esters and Amino alkyl esters of acrylic and methacrylic acid with up to 8 carbon atoms are - if at all - preferably polymerized only in small amounts in the first shell (b2).
  • a monomer mixture becomes a hard second shell (b3), the proportion of which is 5 to 20% by weight, preferably 5 to 15% by weight, of the total weight of the five-stage emulsion graft copolymer, polymerized.
  • the monomer mixture has a composition as indicated for the core material (b 1), which need not, however, be identical to this.
  • the glass transition temperature of the second shell (b3) is generally above 50 ° C, preferably between 80 and 130 ° C.
  • a monomer mixture is polymerized to an elastomeric third shell (b4) in the presence of the three previously polymerized phases.
  • the elastomeric first shell (b2) it has a share of 15 to 50 wt .-%, preferably 20 to 45 wt .-% of the total weight of the graft polymer, with the proviso that the sum of the elastomeric shells (b2) and (b4 ) Is 50 to 75%, preferably 60 to 75% by weight.
  • the total amount of both shells can be distributed equally between the individual elastomeric polymer phases.
  • the monomer mixture used corresponds to a composition according to the shell (b2), but need not be identical to it.
  • the elastomeric third shell (b4) usually has a glass transition temperature below 0 ° C, preferably in the range between -5 and -35 ° C.
  • a monomer mixture is polymerized to an outer hard fourth shell (bgemisch) in the presence of the core and shell latices already formed.
  • the proportion of this shell - also called the outer hard phase - in the total amount of the emulsion graft copolymer is between 15 and 30% by weight, preferably between 15 and 25% by weight, and consists essentially of 80 to 99.95% by weight, preferably 90 to 98.95% by weight of methyl methacrylate (I), 0.05 to 2 wt .-% of a regulator (VII) and 0 to 19.95% by weight, preferably 1 to 9.95% by weight of further monofunctional comonomers (III), wherein as monofunctional comonomers (III) C1-C20 alkyl esters of acrylic acid such as acrylic acid ethyl ester in an amount of 1 to 6 wt .-%, are particularly preferred.
  • monofunctional comonomers (III) C1-C20 alkyl esters of acrylic acid such
  • Monovalent C4-C12 alkyl mercaptans such as sec-butyl mercaptan, n-dodecyl mercaptan and t-dodecyl mercaptan are suitable as regulators (VII).
  • VVII regulators
  • N-Dodecyl mercaptan is particularly suitable.
  • a regulator is of particular importance since it generally limits the chain length in the polymerization of the final phase.
  • the molecular weight of the outer hard phase can be matched to that of the thermoplastic composition, which is particularly advantageous when mixing the emulsion graft copolymers with thermoplastic compositions.
  • the glass transition temperature of the outer shell (b5) is usually greater than 50 ° C, preferably 80 to 130 ° C.
  • the emulsion graft copolymers according to the invention can be prepared in a manner known per se by the method of emulsion graft polymerization, which is also referred to as the seed latex process, in five successive stages, the latex particles generally remaining in the emulsified state until the end stage has been completed.
  • the polymeric product in the seed latex usually determines the total content of particles in the five-stage end product. This means that after the first polymerization stage, further particles are essentially not formed anew and the particle content remains approximately constant.
  • emulsifiers can generally determine the particle size of both the core latex and the latex particles in the intermediate stages, the type and concentration of emulsifier being decisive.
  • Anionogenic and nonionic emulsifiers can be used.
  • Suitable emulsifiers are, for example Dioctyl sodium sulfosuccinate, Sodium lauryl sulfate, Sodium dodecylbenzenesulfonate, Alkylphenoxypolyethylene sulfonates and Salts of long chain carboxylic and sulfonic acids.
  • nonionic emulsifiers are Fatty alcohol polyglycol ether, Alkylaryl polyglycol ether, Fatty acid monoethanolamides as well ethoxylated fatty acid amides and amines suitable.
  • the total amount of emulsifier is preferably 0.05 to 5% by weight.
  • the diameter (d50 value) of the finished emulsion polymer particles is set according to the invention in a manner known per se in the range from 100 to 200 nm, preferably from 100 to 150 nm. In the case of particle sizes of more than 200 nm, it has been observed to date that no low-whitening films (70 ⁇ m thick) are obtained.
  • Ammonium and alkali peroxodisulfates such as potassium peroxodisulfate as well Initiator combination systems such as sodium persulfate-sodium hydrosulfite (sodium dithionite), potassium persulfate-sodium formaldehyde sulfoxylate and potassium peroxodisulfate-sodium dithionite-iron-II-sulfate are used
  • the polymerization temperature in the case of the thermally activated ammonium and alkali metal peroxodisulfates generally being 50 to 100 ° C and in the initiator combinations which are effective as redox systems, may be in the range of about 20 to 50 ° C.
  • the total amount of initiator is preferably between 0.02 and 0.5% by weight, based on the finished emulsion polymer.
  • the polymerization of the core and the other shells can also be carried out in the presence of a regulator.
  • the total amount of regulator is usually between 0.01 and 1 wt .-%, based on the total weight of the polymer.
  • Salts of phosphoric acid e.g. Mixtures of potassium dihydrogen phosphate and disodium hydrogen phosphate; ammoniacal solutions can also be used.
  • the polymerization can be carried out at a temperature in the range between 70 and 100 ° C., a temperature of 85 to 95 ° C. being preferred.
  • the polymerization times are longer at temperatures below 70 ° C, and at temperatures above 100 ° C it is generally necessary to carry out the polymerization under pressure.
  • the emulsion graft copolymer (B) is generally prepared in such a way that an aqueous mixture consisting of monomers, crosslinking agent, emulsifier, initiator, regulator and a buffer system is placed in a reactor inertized with nitrogen, inerted in the cold with stirring and then brings to the polymerization temperature for about 15 to 120 minutes.
  • the core latex is generally first formed by emulsifying and polymerizing the core monomer mixture.
  • the further stages are usually produced in each case with addition of the monomers in the presence of the stage already formed by emulsion polymerization, it being expedient to emulsify the monomers beforehand in an aqueous medium with stirring.
  • the addition of a further stage only takes place when the polymerization of the preceding stage has been completed, as a result of which mixing of the individual stages is suppressed and a pure five-stage structure of the emulsion graft copolymer is ensured.
  • a post-reaction time 15 to 120 minutes after the addition of the respective stage and before the start of the addition of the next stage may be required.
  • the emulsion polymer is isolated from the latex obtained in a known manner by precipitation, filtration and subsequent drying.
  • aqueous solutions of inorganic salts such as sodium chloride, sodium sulfate, magnesium sulfate and calcium chloride
  • aqueous solutions of salts of formic acid such as magnesium formate, calcium formate and zinc formate
  • aqueous solutions of inorganic acids such as sulfuric and phosphoric acid as well as aqueous ammoniacal and amine solutions and others
  • aqueous alkaline solutions such as sodium and potassium hydroxide
  • Drying can be carried out, for example, by freeze, spray, fluidized bed and circulating air drying.
  • the dried polymer can then be processed, for example in extruders with component (A), to give thermoplastic molding compositions.
  • the latex can be coagulated and dewatered directly in the extruder.
  • the latex can also be mixed with component (A) directly in the extruder.
  • the emulsion polymers (B), when mixed with component (A), can be processed to give impact-resistant molded articles, foils and sheets, in particular foils which are used as coating and weather protection layers .
  • other additives such as antioxidants, light stabilizers, thermal stabilizers, lubricants, dyes and fillers can also be processed.
  • thermoplastic molding compositions according to the invention have the advantage over those known from the prior art that they can be processed to give low-whitening films.
  • the emulsion graft copolymers were precipitated from the latices, isolated, washed and dried.
  • the template was heated to 90 ° C. with stirring. After the start of the polymerization, the remainder of the emulsion was metered in within 2 h and then post-polymerized for 1 h. An emulsion was used for the grafting 772.8 g of methyl methacrylate 32.2 g methyl acrylate 3.86 g of n-dodecyl mercaptan metered in within 1 h. The post-polymerization time was 1 hour. The particle size is shown in Table 2.
  • 250 g of the seed latex thus obtained were placed in a stirring apparatus and, as an elastomeric intermediate, a mixture of 91.4 g of n-butyl acrylate, 16.4 g of styrene, 6.5 g of methyl methacrylate and 3.0 g of trimethylolpropane triacrylate and 82 g of water, 09 g of sodium lauryl sulfate and 0.048 g of potassium peroxodisulfate were added and thermally polymerized.
  • a mixture of 80 g methyl methacrylate, 26.5 g water, 0.06 g sodium lauryl sulfate, 0.045 g potassium peroxodisulfate and 0.15 g 2-ethylhexylthioglycolate was then grafted on thermally as the non-elastomeric final stage.
  • the latex had a solids content of 44% by weight.
  • the emulsion polymer was then obtained by spray drying. The particle size is shown in Table 2.
  • Comparative Example 1 was repeated, with the difference that only 1.5 g of trimethylolpropane triacrylate were used in the intermediate stage.
  • the particle size is shown in Table 2.
  • the initial charge was heated to 70 ° C. in a 10 l three-necked flask under nitrogen purging and held at this temperature for 30 min.
  • the solids content was 40% by weight, the average particle diameter was between 160 and 180 nm.
  • thermoplastic molding compositions were produced by compounding on an extruder (ZSK-25, Werner &Pfleiderer; throughput 10 kg / h, 200 rpm and 230 ° C.).
  • thermoplastic molding compositions The susceptibility to whitening of the thermoplastic molding compositions was checked visually on calendered foils (thickness 70 ⁇ m) by bending the foil ten times by 180 ° at one point.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Graft Or Block Polymers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP94111540A 1993-07-31 1994-07-23 Masse à mouler thermoplastique d'un copolymère à base d'alkylesters d'acide méthacrylique et un copolymère greffé à cinq étapes en émulsion Withdrawn EP0636652A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4325823 1993-07-31
DE4325823A DE4325823A1 (de) 1993-07-31 1993-07-31 Thermoplastische Formmassen aus einem Copolymerisat auf der Basis von Alkylestern der Methacrylsäure und einem fünfstufigen Emulsionspfropfcopolymerisat

Publications (1)

Publication Number Publication Date
EP0636652A1 true EP0636652A1 (fr) 1995-02-01

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EP (1) EP0636652A1 (fr)
JP (1) JPH0762192A (fr)
KR (1) KR950003337A (fr)
DE (1) DE4325823A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999044737A1 (fr) * 1998-03-04 1999-09-10 Basf Aktiengesellschaft Procede de production en continu de dispersions de polymeres par polymerisation en emulsion aqueuse
WO2002044290A3 (fr) * 2000-11-30 2003-03-13 Dow Chemical Co Dispersion heteropolymere aqueuse permettant de fabriquer des revetements, et son procede de production
EP0828772B2 (fr) † 1995-05-24 2003-08-20 Ineos Acrylics UK Limited Polymeres (meth)acryliques modifies quant a leur resistance aux chocs
EP0881261B2 (fr) † 1996-02-16 2010-06-30 Sumitomo Chemical Company, Limited Film acrylique et moulages effectues au moyen de ce film
WO2020198179A1 (fr) 2019-03-25 2020-10-01 Arkema France Antichoc haute efficacité et compositions polymères

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100339158B1 (ko) * 1994-12-30 2002-11-23 주식회사 엘지씨아이 열가소성수지조성물의제조방법
KR100431452B1 (ko) * 2001-08-30 2004-05-14 주식회사 엘지화학 메틸메타크릴레이트-부타디엔-스티렌(ｍｂｓ)계 수지의제조방법

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DE2253689A1 (de) * 1971-11-05 1973-05-10 Rohm & Haas Thermoplastische kunststoffmasse
US4180529A (en) * 1977-12-08 1979-12-25 E. I. Du Pont De Nemours And Company Acrylic multistage graft copolymer products and processes
DE3300526A1 (de) * 1983-01-10 1984-07-12 Röhm GmbH, 6100 Darmstadt Schlagzaehmodifizierungsmittel
EP0512333A1 (fr) * 1991-05-04 1992-11-11 BASF Aktiengesellschaft Copolymères greffés en émulsion

Patent Citations (5)

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Publication number Priority date Publication date Assignee Title
DE2253689A1 (de) * 1971-11-05 1973-05-10 Rohm & Haas Thermoplastische kunststoffmasse
US4180529A (en) * 1977-12-08 1979-12-25 E. I. Du Pont De Nemours And Company Acrylic multistage graft copolymer products and processes
DE3300526A1 (de) * 1983-01-10 1984-07-12 Röhm GmbH, 6100 Darmstadt Schlagzaehmodifizierungsmittel
EP0113924A2 (fr) * 1983-01-10 1984-07-25 Röhm Gmbh Agent de modification de la résistance à l'impact
EP0512333A1 (fr) * 1991-05-04 1992-11-11 BASF Aktiengesellschaft Copolymères greffés en émulsion

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0828772B2 (fr) † 1995-05-24 2003-08-20 Ineos Acrylics UK Limited Polymeres (meth)acryliques modifies quant a leur resistance aux chocs
EP0881261B2 (fr) † 1996-02-16 2010-06-30 Sumitomo Chemical Company, Limited Film acrylique et moulages effectues au moyen de ce film
WO1999044737A1 (fr) * 1998-03-04 1999-09-10 Basf Aktiengesellschaft Procede de production en continu de dispersions de polymeres par polymerisation en emulsion aqueuse
WO2002044290A3 (fr) * 2000-11-30 2003-03-13 Dow Chemical Co Dispersion heteropolymere aqueuse permettant de fabriquer des revetements, et son procede de production
WO2020198179A1 (fr) 2019-03-25 2020-10-01 Arkema France Antichoc haute efficacité et compositions polymères
EP3947559A4 (fr) * 2019-03-25 2022-12-07 Trinseo Europe GmbH Antichoc haute efficacité et compositions polymères

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KR950003337A (ko) 1995-02-16
JPH0762192A (ja) 1995-03-07
DE4325823A1 (de) 1995-04-27

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